Transition Metal Complexation in 1,3-Dipolar Cycloadditions

Heterocycles ◽  
2003 ◽  
Vol 59 (2) ◽  
pp. 823 ◽  
Author(s):  
Gaetano Zecchi ◽  
Gianluigi Broggini ◽  
Giorgio Molteni ◽  
Alberto Terraneo
ChemInform ◽  
2003 ◽  
Vol 34 (24) ◽  
Author(s):  
Gianluigi Broggini ◽  
Giorgio Molteni ◽  
Alberto Terraneo ◽  
Gaetano Zecchi

Tetrahedron ◽  
2005 ◽  
Vol 61 (26) ◽  
pp. 6266-6275 ◽  
Author(s):  
Brian M. Bocknack ◽  
Long-Cheng Wang ◽  
Freddie W. Hughes ◽  
Michael J. Krische

1991 ◽  
Vol 113 (13) ◽  
pp. 5059-5060 ◽  
Author(s):  
Keitaro Nishino ◽  
Masanobu Takagi ◽  
Teruhisa Kawata ◽  
Ichiro Murata ◽  
Junji Inanaga ◽  
...  

ChemInform ◽  
2001 ◽  
Vol 32 (8) ◽  
pp. no-no
Author(s):  
Wolfgang W. Schoeller ◽  
Dirk Eisner ◽  
Sonja Grigoleit ◽  
Alexander B. Rozhenko ◽  
Alexander Alijah

1977 ◽  
Vol 99 (25) ◽  
pp. 8366-8367 ◽  
Author(s):  
Yoshihiko Ito ◽  
Toru Sugaya ◽  
Masashi Nakatsuka ◽  
Takeo Saegusa

2020 ◽  
Vol 23 (27) ◽  
pp. 3064-3134 ◽  
Author(s):  
Ana L. Cardoso ◽  
Maria I.L. Soares

The 1,3-dipolar cycloaddition reaction is a powerful and versatile strategy for the synthesis of carbocyclic and heterocyclic five-membered rings. Herein, the most recent developments on the [3+2] cycloaddition reactions using allenes acting either as dipolarophiles or 1,3-dipole precursors, are highlighted. The recent contributions on the phosphine- and transition metal-catalyzed [3+2] annulations involving allenes as substrates are also covered, with the exception of those in which the formation of a 1,3-dipole (or synthetic equivalent) is not invoked. This review summarizes the most relevant research in which allenes are used as building blocks for the construction of structurally diverse five-membered rings via [3+2] annulation reactions.


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